N'-(1-(4-Fluorophenyl)ethylidene)-4-methylbenzenesulfonohydrazide

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Reagent Code: #219205
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CAS Number 75230-49-8

science Other reagents with same CAS 75230-49-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.36 g/mol
Formula C₁₅H₁₅FN₂O₂S
badge Registry Numbers
MDL Number MFCD01353344
thermostat Physical Properties
Boiling Point 432.9±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.23±0.1 g/cm3(Predicted)
Storage 2-8°C, inert atmosphere

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of biologically active compounds. It serves as a building block in the preparation of hydrazone-based derivatives that exhibit antimicrobial, antifungal, and anticancer properties. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its ability to form stable conjugates with carbonyl compounds. Also utilized in the synthesis of sulfonamide-containing heterocycles, which are important scaffolds in drug design. Shows potential in agrochemical research for developing new pesticidal agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,110.00
inventory 1g
10-20 days ฿2,970.00
inventory 5g
10-20 days ฿11,270.00
inventory 25g
10-20 days ฿42,010.00

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N'-(1-(4-Fluorophenyl)ethylidene)-4-methylbenzenesulfonohydrazide
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Used as an intermediate in organic synthesis, particularly in the development of biologically active compounds. It serves as a building block in the preparation of hydrazone-based derivatives that exhibit antimicrobial, antifungal, and anticancer properties. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its ability to form stable conjugates with carbonyl compounds. Also utilized in the synthesis of sulfonamide-containing heterocycles, which are important scaf

Used as an intermediate in organic synthesis, particularly in the development of biologically active compounds. It serves as a building block in the preparation of hydrazone-based derivatives that exhibit antimicrobial, antifungal, and anticancer properties. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its ability to form stable conjugates with carbonyl compounds. Also utilized in the synthesis of sulfonamide-containing heterocycles, which are important scaffolds in drug design. Shows potential in agrochemical research for developing new pesticidal agents.

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